ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "Hematopoietic stem cells"

  • Abstract Number: 072 • 2020 Pediatric Rheumatology Symposium

    Allogenic Hematopoietic Stem Cell Transplantation for Refractory Childhood Rheumatic Diseases

    Camille Beaufils1, Catherine Proulx 2, Annaliesse Blincoe 3, Pierre Teira 4, Henrique Bittencourt 4, Sonia Cellot 5, Michel Duval 4, Johannes Roth 6, Marie-Paule Morin 7, Jean Jacques De Bruycker 7, Julie Couture 7, Kathryn Samaan 8, Helene Decaluwe 7, Fabien Touzot 7, Elie Haddad 7 and Julie Barsalou 7, 1Division of Pediatric Rheumatology-Immunology, CHU Sainte-Justine, Montreal, Quebec, Canada, 2Department of Pediatrics, CHU Sainte-Justine, University of Montreal, Montreal, Quebec, Canada, 3Division of Pediatric Rheumatology-Immunology, CHU Sainte-Justine, Montreal, Canada, 4Division of Pediatric Hematology-Oncology, CHU Sainte-Justine, Department of Pediatrics, University of Montreal, Montreal, Quebec, Canada, 5Division of Pediatric Hematology-Oncology, CHU Sainte-Justine, Department of Pediatrics, University of Montreal, Montreal, Canada, 6Division of Pediatric Rheumatology, Children Hospital of Eastern Ontario, Department of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada, 7Division of Pediatric Rheumatology-Immunology, CHU Sainte-Justine, Department of Pediatrics, University of Montreal, Montreal, Quebec, Canada, 8Division of Pediatric Rheumatology-Immunology,-Allergy, CHU Sainte-Justine, Department of Pediatrics, University of Montreal, Montreal, Quebec, Canada

    Background/Purpose: Patients with refractory rheumatic diseases face poor quality of life, long-term sequelae and life-threatening complications. With advances in allogenic hematopoietic stem cell transplantation (allo-HSCT),…
  • Abstract Number: 2912 • 2019 ACR/ARP Annual Meeting

    Predictive Factors for Treatment Related Mortality and Event-Free Survival After Autologous Hematopoietic Stem Cell Transplantation for Systemic Sclerosis: Results of a Long Term Follow-up Multi-centre Study

    Sandra van Bijnen 1, Maaike Boonstra 2, Els van den Ende 3, Lucia Kroft 2, Bram Geurts 1, Miranda Snoeren 1, Anne Schouffoer 2, Julia Spierings 4, Jacob van Laar 5, Thomas Huizinga 6, Alexandre Voskuyl 7, Walter van der Velden 1, Frank van den Hoogen 3, Jeska de Vries-Bouwstra 6 and Madelon Vonk8, 1Radboud University Nijmegen Medical Centre, Nijmegen, Gelderland, Netherlands, 2Leiden University Medical Centre, Leiden, Zuid-Holland, Netherlands, 3Department of Rheumatology, Radboud University Medical Center, Nijmegen, Gelderland, Netherlands, 4Utrecht Medical Centre, Utrecht, Utrecht, Netherlands, 5UMC Utrecht, Department of Rheumatology & Clinical Immunology, Utrecht, The Netherlands, Utrecht, Netherlands, 6Leiden University Medical Center, Leiden, Netherlands, 7Amsterdam Univiversity Medical Centre, Amsterdam, Noord-Holland, Netherlands, 8Department of Rheumatology, Radboud University Medical Center, Nijmegen, The Netherlands, Nijmegen, Gelderland, Netherlands

    Background/Purpose: Autologous hematopoietic stemcell transplantation (HSCT) has shown to improve survival of SSc patients with poor prognosis, but is hampered by treatment related mortality (TRM).…
  • Abstract Number: 1876 • 2018 ACR/ARHP Annual Meeting

    Machine Learning Classification of Peripheral Blood Gene Expression Identifies a Subset of Patients with Systemic Sclerosis Most Likely to Show Clinical Improvement in Response to Hematopoietic Stem Cell Transplant

    Jennifer Franks1, Viktor Martyanov2, Tammara A. Wood2, Leslie Crofford3, Lynette Keyes-Elstein4, Daniel E. Furst5, Ellen Goldmuntz6, Maureen D. Mayes7, Peter McSweeney8, Richard Nash8, Keith Sullivan9 and Michael L. Whitfield10, 1Geisel School of Medicine at Dartmouth, Hanover, NH, 2Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 3Division of Rheumatology and Immunology, Vanderbilt University Medical Center, Nashville, TN, 4Rho, Inc, Chapel Hill, NC, 5University of California Los Angeles, Los Angeles, CA, 6NIAID, NIH, Bethesda, MD, 7Rheumatology, University of Texas McGovern Medical School, Houston, TX, 8Colorado Blood Cancer Institute, Denver, CO, 9Duke University Medical Center, Durham, NC, 10Biomedical Data Science, Geisel School of Medicine at Dartmouth, Hanover, NH

    Background/Purpose: The SCOT (Scleroderma: Cyclophosphamide or Transplantation) trial (Sullivan K. et al, 2018) demonstrated the clinical benefit of hematopoietic stem cell transplant (HSCT) compared to…
  • Abstract Number: 34 • 2018 ACR/ARHP Annual Meeting

    Microbiome-Drived Aberration of Hematopoietic Stem Cell Development Facilitates Immune Deregulation on the Onset of Collagen-Induced Arthritis in Mice

    Peiqing Yang1, Lingchong Su1, Yanhong Li1, Yi Liu2 and Yubin Luo3, 1West China Hospital, Sichuan University, Chengdu, China, 2Department of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, Sichuan, China, Chengdu, China, 3Department of Rheumatology & Immunology,, West China Hosptial, Sichuan University, Chengdu, China

    Background/Purpose: Increasing studies indicate that immune deregulation occurs prior to symptom in Rheumatoid arthritis (RA). Hematopoietic stem cell (HSC) gives rise to multipotent progenitors differentiating…
  • Abstract Number: 1122 • 2018 ACR/ARHP Annual Meeting

    Lymphocyte Immunophenotypes at Randomization on the Scleroderma: Cyclophosphamide or Transplantation Trial: Comparison of Treatment Naïve and DMARD Treated Participants with Healthy Controls

    Ankoor Shah1, Jan Storek2, Rob Woolson3, Lynette Keyes-Elstein4, Paul Wallace5, Maureen D. Mayes6, Leslie Crofford7, Daniel E. Furst8, Ellen Goldmuntz9, Richard Nash10, Peter McSweeney10 and Keith Sullivan11, 1Medicine, Duke University Medical Center, Durham, NC, 2University of Calgary, Calgary, AB, Canada, 3Rho Inc, Chapel Hill, NC, 4Clinical Statistics, Rho Federal Systems, Inc., Chapel Hill, NC, 5Roswell Park Cancer Institute, Buffalo, NY, 6Rheumatology, University of Texas McGovern Medical School, Houston, TX, 7Division of Rheumatology and Immunology, Vanderbilt University Medical Center, Nashville, TN, 8Medicine, University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 9NIH, Bethesda, MD, 10Colorado Blood Cancer Institute, Denver, CO, 11Duke University Medical Center, Durham, NC

    Background/Purpose: The Scleroderma:Cyclophosphamide or Transplantation Trial (SCOT) study compared stem cell transplant to monthly cyclophosphamide (CYC) in patients with scleroderma (SSc). We studied baseline lymphocyte…
  • Abstract Number: 1820 • 2018 ACR/ARHP Annual Meeting

    Myeloablative Autologous Hematopoietic Stem Cell Transplantation for Severe Scleroderma: Long-Term Outcomes 6-11 Years after Entry on a Randomized Study Comparing Transplantation and Cyclophosphamide

    Keith Sullivan1, Ashley Pinckney2, Ellen Goldmuntz3, Beverly Welch4, Dinesh Khanna5, Robert W. Simms6, Suzanne Kafaja7, George Georges8, Jan Storek9, Mary Ellen Csuka10, Richard Nash11, Daniel E. Furst12, Leslie Crofford13, Peter McSweeney11, Maureen D. Mayes14 and Lynette Keyes-Elstein15, 1Duke University Medical Center, Durham, NC, 2Rho Federal Systems, Inc., Chapel Hill, NC, 3NIAID, NIH, Bethesda, MD, 4National Institutes of Health, Bethesda, MD, 5Division of Rheumatology, Department of Internal Medicine, University of Michigan Scleroderma Program, University of Michigan, Ann Arbor, MI, 6Rheumatology, Boston University School of Medicine, Boston, MA, 7David Geffen School of Medicine, UCLA, Los Angeles, CA, 8Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA, 9University of Calgary, Calgary, AB, Canada, 10Medicine, Medical College of Wisconsin, Milwaukee, WI, 11Colorado Blood Cancer Institute, Denver, CO, 12University of Washington, Seattle, WA, 13Division of Rheumatology and Immunology, Vanderbilt University Medical Center, Nashville, TN, 14Rheumatology, University of Texas McGovern Medical School, Houston, TX, 15Clinical Statistics, Rho Federal Systems, Inc., Chapel Hill, NC

    Background/Purpose: The Scleroderma: Cyclophosphamide or Transplantation (SCOT) trial demonstrated that for adults with severe scleroderma (ACR 1995 criteria) and internal organ involvement, myeloablative CD34+selected autologous…
  • Abstract Number: 4 • 2017 Pediatric Rheumatology Symposium

    Microbiota-Dependent Signals Regulate Inflammatory Myelopoiesis in a Murine Model of Macrophage Activation Syndrome

    Lehn K. Weaver1, Chhanda Biswas1, Niansheng Chu1 and Edward M. Behrens2, 1Pediatric Rheumatology, Children's Hospital of Philadelphia, Philadelphia, PA, 2Rheumatology, Children's Hospital of Philadelphia, Philadelphia, PA

    Background/Purpose: Targeting host-microbiota interactions to limit production of pathogenic myeloid cells that fuel chronic inflammatory responses is of therapeutic interest. Recent evidence suggests that this may…
  • Abstract Number: 6L • 2016 ACR/ARHP Annual Meeting

    Myeloablative Autologous Transplantation of CD34+ -Selected Hematopoietic Stem Cells (HSCT) Vs Monthly Intravenous Cyclophosphamide (CYC) for Severe Scleroderma with Internal Organ Involvement: Outcomes of a Randomized North American Clinical Trial

    Keith Sullivan1, Lynette Keyes-Elstein2, Peter McSweeney3, Ashley Pinckney2, Beverly Welch4, Maureen D Mayes5, Richard Nash3, Leslie J. Crofford6, Sharon Castina2, Linda Griffith7, Ellen Goldmuntz8 and Daniel E. Furst9, 1Duke University, Durham, NC, 2Rho, Inc, Chapel Hill, NC, 3Colorado Blood Cancer Institute, Denver, CO, 46610 Rockledge Dr., NIAID/NIH, Bethesda, MD, 5Department of Internal Medicine - Rheumatology, University of Texas-McGovern Medical School, Houston, TX, 6Medicine, Vanderbilt University Medical Center, Nasville, TN, 7NIAID, NIH, Bethesda, MD, 8NIAID, National Institutes of Health, Bethesda, MD, 9David Geffen School of Medicine at UCLA, Los Angeles, CA

      Background/Purpose: Therapeutic options for diffuse cutaneous systemic sclerosis (dcSSc) are limited. The Scleroderma: Cyclophosphamide or Transplantation (SCOT) trial was a multicenter study designed to…
  • Abstract Number: 1369 • 2015 ACR/ARHP Annual Meeting

    Enhanced Myelopoiesis Downstream of Toll-like Receptor 9 Activation Drives a Feed-Forward Inflammatory Response

    Lehn K. Weaver1 and Edward M. Behrens2, 1Pediatric Rheumatology, Children's Hospital of Philadelphia, Philadelphia, PA, 2Pediatric Rheumatology, Childrens Hospital of Philadelphia, Philadelphia, PA

    Background/Purpose: Monocytes are myeloid cells important for the initiation of inflammation and have been implicated in the pathogenesis of autoimmunity. Monocytes interact with their environment…
  • Abstract Number: 2168 • 2014 ACR/ARHP Annual Meeting

    Extramedullary Myelopoiesis Drives Persistent Toll-like Receptor-Mediated Inflammation

    Lehn K. Weaver1 and Edward M. Behrens2, 1Pediatric Rheumatology, Children's Hospital of Philadelphia, Philadelphia, PA, 2Pediatric Rheumatology, Childrens Hospital of Philadelphia, Philadelphia, PA

    Background/Purpose: Many rheumatic diseases are driven by chronic, repeated activation of Toll-like receptors (TLR) causing the initiation and perpetuation of disease. However, TLR-activated innate immune…
  • Abstract Number: 1610 • 2013 ACR/ARHP Annual Meeting

    Lymphoablation Including B Cell Depletion and Autologous Hematopoietic Stem Cell Transplantation Leads To Long Remissions In Treatment-Resistant Systemic Lupus Erythematosus Patients

    Sarfaraz A. Hasni1, Gabor G. Illei2, Nikolay P. Nikolov3, Francis Hakim4, Susan Leitman4, James E. Balow5, Howard A. Austin6, Juan Gea-Banacloche4, Unsong Oh7, Paulo Muraro8, Claude Sportes9, Peter E. Lipsky10, Ronald Gress9, Steve Pavletic9 and Amrie Grammer11, 1National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 2Sjogren's Clinic, NIDCR/ NIH, Bethesda, MD, 3NIDCR, NIH, Bethesda, MD, 4NCI, NIH, Bethesda, MD, 5Clinical Director, NIDDK, National Institutes of Health, Bethesda, MD, 6Kidney Disease Section, NIDDK/NIH, Bethesda, MD, 7NINDS, NIH, Bethesda, MD, 8NINDS/NIH, Bethesda, MD, 9NCI/NIH, Bethesda, MD, 10NIAMS/NIH, Bethesda, MD, 11AMPEL BioSolutions, Charlottesville, VA

    Background/Purpose: Over the past two decades, approximately 200 patients with severe systemic lupus erythematosus(SLE) have received autologous hematopoietic stem cell transplants (autoHSCT). More than half…
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology